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U heeft gezocht op: 2,3,5-Triiodobenzoic+acid


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2,3,5-Trifluorobenzoic acid 98%

Leverancier: Apollo Scientific
Omschrijving: 2,3,5-Trifluorobenzoic acid 98%

Image Unavailable-ICNA0210290880

Sodium diatrizoate ≥99%, white crystalline powder

Leverancier: MP Biomedicals
Omschrijving: Sodium Diatrizoate has been shown to cause partial redistribution of tight-junction-associated membrane proteins into a cytoplasmic compartment in cultured monolayer MDCK cells.

Image Unavailable-APOSBICL4287-1G

2,3,5-Tri-O-acetyl-D-xylonic acid, γ-lactone ≥98%

Leverancier: Apollo Scientific
Omschrijving: 2,3,5-Tri-O-acetyl-D-xylonic acid, γ-lactone ≥98%

Product Image-84756.180

UV-VIS-lineariteitsstandaarden voor spectroscopie bij 235, 257, 313 en 350 nm

Catalogus nummer: (84756.180)
Leverancier: VWR Chemicals
Omschrijving: Lineariteitsstandaarden verpakt in permanent afgedichte UV-cuvetten of bruine flessen van 100 ml.
UOM: 1 * 100 mL

MSDS Certificaten


Image Unavailable-BWRLBS2737

Anti-NMBR Rabbit Polyclonal Antibody [clone: L264]

Catalogus nummer: (BWRLBS2737)
Leverancier: Bioworld Technology
Omschrijving: Synthetic peptide, corresponding to amino acids 235-280 of Human NMBR.
UOM: 1 * 1 EA
Image Unavailable-BWRLBS3796

Anti-ACAT1 Rabbit Polyclonal Antibody [clone: K266]

Catalogus nummer: (BWRLBS3796)
Leverancier: Bioworld Technology
Omschrijving: Synthetic peptide, corresponding to amino acids 235-286 of Human ACAT1.
UOM: 1 * 1 EA
Image Unavailable-BOSSBS-13623R-A555

Anti-TMEM176A Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalogus nummer: (BOSSBS-13623R-A555)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13623R-CY7

Anti-TMEM176A Rabbit Polyclonal Antibody (Cy7®)

Catalogus nummer: (BOSSBS-13623R-CY7)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13623R-A647

Anti-TMEM176A Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalogus nummer: (BOSSBS-13623R-A647)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13623R-CY5

Anti-TMEM176A Rabbit Polyclonal Antibody (Cy5®)

Catalogus nummer: (BOSSBS-13623R-CY5)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13623R-CY3

Anti-TMEM176A Rabbit Polyclonal Antibody (Cy3®)

Catalogus nummer: (BOSSBS-13623R-CY3)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13623R-A350

Anti-TMEM176A Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Catalogus nummer: (BOSSBS-13623R-A350)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13623R

Anti-TMEM176A Rabbit Polyclonal Antibody

Catalogus nummer: (BOSSBS-13623R)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13623R-A488

Anti-TMEM176A Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Catalogus nummer: (BOSSBS-13623R-A488)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13623R-HRP

Anti-TMEM176A Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalogus nummer: (BOSSBS-13623R-HRP)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13623R-FITC

Anti-TMEM176A Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalogus nummer: (BOSSBS-13623R-FITC)
Leverancier: Bioss
Omschrijving: TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
UOM: 1 * 100 µl
Bel voor prijs
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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